MedPath

PEITEL 2,5 MG/G UNGUENTO

PEITEL 2,5 MG/G UNGUENTO

Pending
Register Number

60371

Prescription Type

Medicamento Sujeto A Prescripción Médica

Authorization Date

Nov 30, 1994

Dosage Form

POMADA

Route: USO CUTÁNEO

Product Details

Detailed information about this CIMA AEMPS approved pharmaceutical product.

Basic Information

Key regulatory and product classification details

Regulatory Details

Register Number60371
EMA Approved
No

Drug Classification

Generic
No
Orphan
No
Biosimilar
No
Commercialized
No
CIMA AEMPS Classification

INGREDIENTS (1)

PREDNICARBATOActive
Quantity: 0,250 g
Name: PREDNICARBATO

ATC CLASSIFICATION (3)

D07A
D07AC
D07AC18

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.